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Vicoprofen
Vicoprofen - 54868-4035-1 - (Hydrocodone Bitartrate and Ibuprofen)
Drug Information of Vicoprofen
| Product NDC: | 54868-4035 |
| Proprietary Name: | Vicoprofen |
| Non Proprietary Name: | Hydrocodone Bitartrate and Ibuprofen |
| Active Ingredient(s): | 7.5; 200 mg/1; mg/1 & nbsp; Hydrocodone Bitartrate and Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vicoprofen
| Product NDC: | 54868-4035 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020716 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980513 |
Package Information of Vicoprofen
| Package NDC: | 54868-4035-1 |
| Package Description: | 20 TABLET, COATED in 1 BOTTLE (54868-4035-1) |
NDC Information of Vicoprofen
| NDC Code | 54868-4035-1 |
| Proprietary Name | Vicoprofen |
| Package Description | 20 TABLET, COATED in 1 BOTTLE (54868-4035-1) |
| Product NDC | 54868-4035 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Ibuprofen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980513 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | HYDROCODONE BITARTRATE; IBUPROFEN |
| Strength Number | 7.5; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
